Evaluation of the postoperative clinical and fluoroscopical outcome of Episealer-Kneeimplants

Not Applicable

• Conditions: Knee Arthroplasty; Z96.6; Presence of orthopaedic joint implants

• Registration Number: DRKS00020586
• Lead Sponsor: Julius Wolff Institut & Berlin-Brandenburg Center for Regenerative Therapies Charité - Universitätsmedizin Berlin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-01-30
• Study Completion: 2020-04-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 9

Inclusion Criteria

•Indication for a knee arthroplasty after primary and secondary knee osteoarthritis
•Patient agreement to participate in the study
•Implantation of the previously described designs

Exclusion Criteria

Patients with contra indications to knee arthroplasty

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Fluoroscopic examination of the knee joint kinematics in patients with episealer implants at 12 months postoperative

Secondary Outcome Measures

Name	Time	Method
Examination of the knee joint Range of motion (RoM) with a goniometer and collection of the clinical data with the questionnaires KSS, High flexion knee score and Forgotten joint score preoperative and after 12 months postoperative.